Ikeda_2002_J.Biosci.Bioeng_93_98

Reference

Title : Enantioselective esterification of racemic ibuprofen in isooctane by immobilized lipase on cellulose acetate-titanium iso-propoxide gel fiber - Ikeda_2002_J.Biosci.Bioeng_93_98
Author(s) : Ikeda Y , Kurokawa Y
Ref : J Biosci Bioeng , 93 :98 , 2002
Abstract :

Lipase (Candida rugosa) was entrap-immobilized on cellulose acetate-titanium iso-propoxide gel fiber by the sol-gel method. The immobilized lipase was used for the direct synthesis of (S)-ibuprofen ester from racemic ibuprofen using propyl alcohol as an acyl acceptor in isooctane. The activity of the immobilized lipase was decreased to about 10-20% that of native lipase. However, the reaction was more enantioselective compared to that with native lipase. The stability for repeated use was improved by immobilization.

PubMedSearch : Ikeda_2002_J.Biosci.Bioeng_93_98
PubMedID: 16233173

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Citations formats

Ikeda Y, Kurokawa Y (2002)
Enantioselective esterification of racemic ibuprofen in isooctane by immobilized lipase on cellulose acetate-titanium iso-propoxide gel fiber
J Biosci Bioeng 93 :98

Ikeda Y, Kurokawa Y (2002)
J Biosci Bioeng 93 :98